Arbeitsgruppe Ruckdeschel
The interaction of microbial pathogens with host cells critically determines the genesis of infectious diseases. When faced with a bacterial pathogen the multicellular organism raises a series of defense responses involving both innate and adaptive immunity. Professional phagocytes, such as neutrophils and resident macrophages, largely constitute the first line innate cellular host defense. They directly attack invading pathogens, mediate the secretion of pro-inflammatory cytokines and mount a protective immune response. Bacterial pathogens on the contrary have evolved sophisticated strategies for the evasion and neutralization of host defense mechanisms. A prototypical pathogen for the subversion of host immune responses is given by the gram-negative enteropathogenic bacterium Yersinia enterocolitica. Our group is exploring the bidirectional crosstalk between Yersinia enterocolitica and its cellular host. Our studies aim to uncover the molecular mechanisms of Yersinia-mediated immunomodulation that enable the establishment of disease.
This work is supported by grants from the Deutsche Forschungsgemeinschaft DFG.
| Position | Name | Phone | Fax | |
|---|---|---|---|---|
| Group leader | PD Dr. med. K. Ruckdeschel | 58184 | 53250 | k.ruckdeschel@uke.de |
| MTA | N. Cymmeck | 54663 | 53250 | n.cymmeck@uke.de |
| Graduate student | Cand. med. C. Fenner | 54663 | 53250 | c.fenner@uke.de |
| Graduate student | Dipl. Biol. L. Novikova | 54663 | 53250 | l.novikova@uke.de |
Exploring the impact of Yersinia effector proteins on inflammatory and apoptotic signal transduction processes
Gram-negative, pathogenic bacteria from the genus Yersinia engage a type III protein secretion system that delivers a set of virulence proteins, the so-called Yops (Yersinia outer proteins), inside eukaryotic cells. There, the Yops perturb key cellular signal transduction pathways of innate immunity. This renders infected cells unable to respond adequately to bacterial infection. The Yersinia Yops act at several cellular levels to suppress multiple programmed anti-bacterial effector functions. Accordingly, the Yop activities counteract phagocytosis, suppress pro-inflammatory activities and trigger apoptosis in macrophages.
Our group is analyzing different molecular aspects in the crosstalk of Yersinia with host cells. We focus on the impact of Y. enterocolitica virulence traits on cellular signal transduction processes that are related to host defense mechanisms.
In particular, the following issues are currently under investigation:J774A.1 macrophages undergoing apoptosis 6 h after onset of Y. enterocolitica infection.
 |
 |
 |
 |
| Wildtype strain | Avirulent strain |
Macrophages infected with the wild type strain display a heterogeneous, apoptotic morphology in phase-contrast microscopy (left). In a portion of the dying cells, apoptosis-typical DNA-fragmentation and nuclear condensation are detected by TUNEL-labeling of free DNA fragments with fluorescein (right). These apoptotic features are not observed in cells infected an avirulent Yersinia strain defective in type III secretion.
Deuretzbacher A, Czymmeck N, Reimer R, Trülzsch K, Gaus K, Hohenberg H, Heesemann J, Aepfelbacher M, Ruckdeschel K.
Beta1 integrin-dependent engulfment of Yersinia enterocolitica by macrophages is coupled to the activation of autophagy and suppressed by type III protein secretion.
J Immunol. 2009 Nov 1;183(9):5847-60. Epub 2009 Oct 7.
Ruckdeschel K, Deuretzbacher A, Haase R.
Crosstalk of signalling processes of innate immunity with Yersinia Yop effector functions.
Immunobiology. 2008;213(3-4):261-9.
Hentschke M, Trülzsch K, Heesemann J, Aepfelbacher M, Ruckdeschel K.
Serogroup-related escape of Yersinia enterocolitica YopE from degradation by the ubiquitin-proteasome pathway.
Infect Immun. 2007 Sep;75(9):4423-31.
Ruckdeschel K, Pfaffinger G, Trülzsch K, Zenner G, Richter K, Heesemann J, Aepfelbacher M.
The proteasome pathway destabilizes Yersinia outer protein E and represses its antihost cell activities.
J Immunol. 2006 May 15;176(10):6093-102.
Haase R, Richter K, Pfaffinger G, Courtois G, Ruckdeschel K.
Yersinia outer protein P suppresses TGF-beta-activated kinase-1 activity to impair innate immune signaling in Yersinia enterocolitica-infected cells.
J Immunol. 2005 Dec 15;175(12):8209-17.
 |
Kontakt |
